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3-Bromo-2-fluoropyridine

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Products Intro: Product Name:3-Bromo-2-fluoropyridine
CAS:36178-05-9
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Products Intro: Product Name:3-Bromo-2-fluoropyridine
CAS:36178-05-9
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CAS:36178-05-9
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Products Intro: Product Name:3-Bromo-2-fluoropyridine
CAS:36178-05-9
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Products Intro: Product Name:3-Bromo-2-fluoropyridine
CAS:36178-05-9

3-Bromo-2-fluoropyridine manufacturers

3-Bromo-2-fluoropyridine Basic information
Product Name:3-Bromo-2-fluoropyridine
Synonyms:2-fluoro-3-bromopyridine;broMo-3 fluoro-2 pyridine;2--3-pyridyl broMidefluoride;2-fluoro -3-pyridyl broMide;3-BROMO-2-FLUOROPYRIDINE;3-Bromo-3-Fluoropyridine;3-Bromo-2-fluoropyridine >;3-Bromo-2-fL
CAS:36178-05-9
MF:C5H3BrFN
MW:175.99
EINECS:672-944-7
Product Categories:blocks;Bromides;FluoroCompounds;Pyridines;Pyridine;Pyridine series;Fluorine series;Halides;Variety of halogenated heterocyclic series;Fluorin-contained pyridine series
Mol File:36178-05-9.mol
3-Bromo-2-fluoropyridine Structure
3-Bromo-2-fluoropyridine Chemical Properties
Boiling point 76°C
density 1.729
refractive index 1.5370-1.5410
Fp 54℃
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka-2.79±0.10(Predicted)
form clear liquid
color Colorless to Light yellow
CAS DataBase Reference36178-05-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 22-37/38-41
Safety Statements 26-39
RIDADR 2810
HazardClass 6.1
HazardClass IRRITANT
PackingGroup 
HS Code 29333990
MSDS Information
3-Bromo-2-fluoropyridine Usage And Synthesis
Chemical PropertiesLight yellow liquid
Synthesis
3-Bromo-2-chloropyridine

52200-48-3

3-Bromo-2-fluoropyridine

36178-05-9

GENERAL METHOD: 2,3-Dichloropyridine (1.00 g, 6.76 mmol) was dissolved in DMSO (33.8 mL) at room temperature, followed by the addition of CsF (2.053 g, 13.51 mmol). The reaction mixture was stirred at 110 °C for 20 h in air. Upon completion of the reaction, the reaction mixture was quenched with ice water and extracted with EtOAc. The organic layer was separated, washed sequentially with water and brine, dried over anhydrous Na2SO4 and subsequently concentrated under reduced pressure. Purification of the residue by column chromatography (silica gel as stationary phase and EtOAc in hexane as eluent) afforded 3-chloro-2-fluoropyridine (0.639 g, 4.86 mmol, 71.9% yield) as a colorless oil. Compounds 3B'-8B' were prepared by a method similar to the synthetic procedure described above for 2B'.

References[1] Tetrahedron Letters, 2015, vol. 56, # 44, p. 6043 - 6046
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